CD1, Antigen, Biochemistry, T cell and Antigen presentation are his primary areas of study. His studies deal with areas such as T lymphocyte, Cell biology and MHC restriction, T-cell receptor as well as CD1. His work focuses on many connections between Antigen and other disciplines, such as Immune system, that overlap with his field of interest in Epitope.
As a part of the same scientific study, he usually deals with the Biochemistry, concentrating on Lipoarabinomannan and frequently concerns with Intracellular parasite, ATP synthase and Mannose. His T cell study is concerned with Genetics in general. D. Branch Moody does research in Antigen presentation, focusing on Antigen processing specifically.
His primary scientific interests are in Antigen, CD1, Biochemistry, T cell and Cell biology. The various areas that D. Branch Moody examines in his Antigen study include Receptor and Immune system. His study in CD1 is interdisciplinary in nature, drawing from both CD1D, T-cell receptor, Major histocompatibility complex and Antigen presentation.
His biological study spans a wide range of topics, including Mycobacterium tuberculosis and Mycolic acid. D. Branch Moody has researched T cell in several fields, including Cytotoxic T cell, T lymphocyte and Microbiology. The study incorporates disciplines such as Cell and In vivo in addition to Cell biology.
His primary areas of investigation include Mycobacterium tuberculosis, T-cell receptor, Antigen, Cell biology and Major histocompatibility complex. His Mycobacterium tuberculosis study combines topics in areas such as Antibiotics, Immunology, Heritability, In silico and Virulence. His studies examine the connections between T-cell receptor and genetics, as well as such issues in Receptor, with regards to Lipid antigen, Tissue damage and Glycolipid.
The Antigen study combines topics in areas such as T cell and Mycolic acid. Many of his studies on Major histocompatibility complex apply to CD1 as well. His research in CD1 tackles topics such as Antigen presentation which are related to areas like CD1D.
The scientist’s investigation covers issues in Mycobacterium tuberculosis, Antigen, Major histocompatibility complex, CD1 and Immune system. His studies in Mycobacterium tuberculosis integrate themes in fields like Biochemistry, Antibiotics, Serine and Biosynthesis. CD1 is closely attributed to T-cell receptor in his study.
His T-cell receptor study integrates concerns from other disciplines, such as Receptor, Cell biology, Epitope, Antigen presentation and In vivo. His studies deal with areas such as Molecular biology, Mycobacterium bovis and Mycolic acid as well as Immune system. His work in T cell tackles topics such as Allergic contact dermatitis which are related to areas like Microbiology.
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The burgeoning family of unconventional T cells.
Dale I Godfrey;Dale I Godfrey;Adam P Uldrich;Adam P Uldrich;James McCluskey;Jamie Rossjohn;Jamie Rossjohn;Jamie Rossjohn.
Nature Immunology (2015)
CD1c-mediated T-cell recognition of isoprenoid glycolipids in Mycobacterium tuberculosis infection
D. Branch Moody;Timo Ulrichs;Timo Ulrichs;Walter Mühlecker;David C. Young.
Structural requirements for glycolipid antigen recognition by CD1b-restricted T cells.
D. Branch Moody;Bruce B. Reinhold;Mark R. Guy;Evan M. Beckman.
Apolipoprotein-mediated pathways of lipid antigen presentation
Peter van den Elzen;Salil Garg;Luis León;Manfred Brigl.
Interpreting expression data with metabolic flux models: predicting Mycobacterium tuberculosis mycolic acid production.
Caroline Colijn;Caroline Colijn;Caroline Colijn;Aaron Brandes;Jeremy Daniel Hofeld Zucker;Desmond S. Lun;Desmond S. Lun.
PLOS Computational Biology (2009)
The Mycobacterium tuberculosis regulatory network and hypoxia.
James E. Galagan;Kyle J. Minch;Matthew Peterson;Anna Lyubetskaya.
Mycobacterial Esx-3 is required for mycobactin-mediated iron acquisition
M. Sloan Siegrist;Meera Unnikrishnan;Matthew J. McConnell;Mark Borowsky.
Proceedings of the National Academy of Sciences of the United States of America (2009)
T cell activation by lipopeptide antigens.
D. Branch Moody;David C. Young;Tan-Yun Cheng;Jean-Pierre Rosat.
Intracellular pathways of CD1 antigen presentation.
D. Branch Moody;Steven A. Porcelli.
Nature Reviews Immunology (2003)
CD1a-autoreactive T cells are a normal component of the human αβ T cell repertoire
Annemieke de Jong;Victor Peña-Cruz;Tan-Yun Cheng;Rachael A Clark.
Nature Immunology (2010)
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